A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18079061



Internal ID20646102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:146785987..146806010hg38UCSC Ensembl
chr2:147543555..147563578hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg3820024
hg1920024
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6344154
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18079061
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer